Method and apparatus for attaching connective tissues to bone using a cortical bone anchoring device

ABSTRACT

A bone anchor device for attaching connective tissue to bone comprises a disk adapted for insertion into a portion of bone to which the connective tissue is to be attached. The disk is movable between a bent orientation for presenting a smaller cross-section and an expanded orientation for presenting a larger cross-section. The bent orientation is utilized for inserting the disk through a small hole into a region of cancellous bone beneath the cortical bone layer, after which the disk is actuated to its expanded orientation so that it will be permanently anchored in the cancellous bone, as it will be too large to return proximally through the hole in the cortical bone layer. Two embodiments are disclosed. In a first embodiment, the disk is initially formed in the expanded orientation, of spring steel. In a second embodiment, the disk is initially formed in the bent orientation, and spring steel is not required.

BACKGROUND OF THE INVENTION

[0001] This invention relates generally to methods and apparatus forattaching soft tissue to bone, and more particularly to anchors andmethods for securing connective tissue, such as ligaments or tendons, tobone. The invention has particular application to arthroscopic surgicaltechniques for reattaching the rotator cuff to the humeral head, inorder to repair the rotator cuff.

[0002] It is an increasingly common problem for tendons and other soft,connective tissues to tear or to detach from associated bone. One suchtype of tear or detachment is a “rotator cuff” tear, wherein thesupraspinatus tendon separates from the humerus, causing pain and lossof ability to elevate and externally rotate the arm. Complete separationcan occur if the shoulder is subjected to gross trauma, but typically,the tear begins as a small lesion, especially in older patients.

[0003] To repair a torn rotator cuff, the typical course today is to doso surgically, through a large incision. This approach is presentlytaken in almost 99% of rotator cuff repair cases. There are two types ofopen surgical approaches for repair of the rotator cuff, one known asthe “classic open” and the other as the “mini-open”. The classic openapproach requires a large incision and complete detachment of thedeltoid muscle from the acromion to facilitate exposure. The cuff isdebrided to ensure suture attachment to viable tissue and to create areasonable edge approximation. In addition, the humeral head is abradedor notched at the proposed soft tissue to bone reattachment point, ashealing is enhanced on a raw bone surface. A series of small diameterholes, referred to as “transosseous tunnels”, are “punched” through thebone laterally from the abraded or notched surface to a point on theoutside surface of the greater tuberosity, commonly a distance of 2 to 3cm. Finally, the cuff is sutured and secured to the bone by pulling thesuture ends through the transosseous tunnels and tying them togetherusing the bone between two successive tunnels as a bridge, after whichthe deltoid muscle must be surgically reattached to the acromion.Because of this maneuver, the deltoid requires postoperative protection,thus retarding rehabilitation and possibly resulting in residualweakness. Complete rehabilitation takes approximately 9 to 12 months.

[0004] The mini-open technique, which represents the current growingtrend and the majority of all surgical repair procedures, differs fromthe classic approach by gaining access through a smaller incision andsplitting rather than detaching the deltoid. Additionally, thisprocedure is typically performed in conjunction with arthroscopicacromial decompression. Once the deltoid is split, it is retracted toexpose the rotator cuff tear. As before, the cuff is debrided, thehumeral head is abraded, and the so-called “transosseous tunnels”, are“punched” through the bone or suture anchors are inserted. Following thesuturing of the rotator cuff to the humeral head, the split deltoid issurgically repaired.

[0005] Although the above described surgical techniques are the currentstandard of care for rotator cuff repair, they are associated with agreat deal of patient discomfort and a lengthy recovery time, rangingfrom at least four months to one year or more. It is the above describedmanipulation of the deltoid muscle together with the large skin incisionthat causes the majority of patient discomfort and an increased recoverytime.

[0006] Less invasive arthroscopic techniques are beginning to bedeveloped in an effort to address the shortcomings of open surgicalrepair. Working through small trocar portals that minimize disruption ofthe deltoid muscle, a few surgeons have been able to reattach therotator cuff using various bone anchor and suture configurations. Therotator cuff is sutured intracorporeally and an anchor is driven intobone at a location appropriate for repair. Rather than thread the suturethrough transosseous tunnels which are difficult or impossible to createarthroscopically using current techniques, the repair is completed bytying the cuff down against bone using the anchor and suture. Earlyresults of less invasive techniques are encouraging, with a substantialreduction in both patient recovery time and discomfort.

[0007] Unfortunately, the skill level required to facilitate an entirelyarthroscopic repair of the rotator cuff is inordinately high.Intracorporeal suturing is clumsy and time consuming, and only thesimplest stitch patterns can be utilized. Extracorporeal knot tying issomewhat less difficult, but the tightness of the knots is difficult tojudge, and the tension cannot later be adjusted. Also, because of theuse of bone anchors to provide a suture fixation point in the bone, theknots that secure the soft tissues to the anchor by necessity leave theknot bundle on top of the soft tissues. In the case of rotator cuffrepair, this means that the knot bundle is left in the shoulder capsulewhere it is able to be felt by the patient postoperatively when thepatient exercises the shoulder joint. So, knots tied arthroscopicallyare difficult to achieve, impossible to adjust, and are located in lessthan optimal areas of the shoulder. Suture tension is also impossible tomeasure and adjust once the knot has been fixed. Consequently, becauseof the technical difficulty of the procedure, presently less than 1% ofall rotator cuff procedures are of the arthroscopic type, and areconsidered investigational in nature.

[0008] Another significant difficulty with current arthroscopic rotatorcuff repair techniques are shortcomings related to currently availablesuture anchors. Suture eyelets in bone anchors available today, whichlike the eye of a needle are threaded with the thread or suture, aresmall in radius, and can cause the suture to fail at the eyelet when theanchor is placed under high tensile loads.

[0009] There are various bone anchor designs available for use by anorthopedic surgeon for attachment of soft tissues to bone. The basiccommonality between the designs is that they create an attachment pointin the bone for a suture that may then be passed through the softtissues and tied, thereby immobilizing the soft tissue. This attachmentpoint may be accomplished by different means. Screws are known forcreating such attachments, but suffer from a number of disadvantages,including their tendency to loosen over time, requiring a secondprocedure to later remove them, and their requirement for a relativelyflat attachment geometry.

[0010] Another approach is to utilize the difference in density in thecortical bone (the tough, dense outer layer of bone) and the cancellousbone (the less dense, airy and somewhat vascular interior of the bone).There is a clear demarcation between the cortical bone and cancellousbone, where the cortical bone presents a kind of hard shell over theless dense cancellous bone. The aspect ratio of the anchor is such thatit typically has a longer axis and a shorter axis and usually ispre-threaded with a suture. These designs use a hole in the corticalbone through which an anchor is inserted. The hole is drilled such thatthe shorter axis of the anchor will fit through the diameter of thehole, with the longer axis of the anchor being parallel to the axis ofthe drilled hole. After deployment in to the cancellous bone, the anchoris rotated 90° so that the long axis is aligned perpendicularly to theaxis of the hole. The suture is pulled, and the anchor is seated upagainst the inside surface of the cortical layer of bone. Due to themismatch in the dimensions of the long axis of the anchor and the holediameter, the anchor cannot be retracted proximally from the hole, thusproviding resistance to pull-out. These anchors still suffer from theaforementioned problem of eyelet design that stresses the sutures.

[0011] Still other prior art approaches have attempted to use a “poprivet” approach. This type of design requires a hole in the corticalbone into which a split shaft is inserted. The split shaft is hollow,and has a tapered plug leading into its inner lumen. The tapered plug isextended out through the top of the shaft, and when the plug isretracted into the inner lumen, the tapered portion causes the splitshaft to be flared outwardly, ostensibly locking the device into thebone.

[0012] Other methods of securing soft tissue to bone are known in theprior art, but are not presently considered to be feasible for shoulderrepair procedures, because of physicians' reluctance to leave anythingbut a suture in the capsule area of the shoulder. The reason for this isthat staples, tacks, and the like could possibly fall out and causeinjury during movement. As a result of this constraint, the attachmentpoint often must be located at a less than ideal position. Also, thetacks or staples require a substantial hole in the soft tissue, and makeit difficult for the surgeon to precisely locate the soft tissuerelative to the bone.

[0013] An approach that also utilizes the difference in density betweenthe cortical and cancellous layers of bone is described in U.S. Pat. No.5,618,314 to Harwin, et al. In that design, the anchor device usesstationary wing members which extend proximally and radially outwardfrom the anchor member and which employ a cutting means along the wingmembers. In this approach, the anchor device is inserted into a holewhich has been drilled into the bone and then rotated radially such thatthe wing members with the cutting means are disposed into the cancellouslayer of bone just below the cortical bone. With this device, arelatively small surface area of the wing members are disposed againstthe cortical bone in comparison with the present invention, making itmore prone to being pulled out of the bone structure as proximal tensionis applied to the suture.

[0014] A number of other various methods of anchoring a suture to boneutilizing the difference in density between the cortical and cancellousbone are described in U.S. Pat. No. 5,417,691 to Hayhurst. One suchmethod describes an anchor with a series of proximally pointing barbsalong its member, which is inserted, into a hole in the bone structure,utilizing the barbs as a means of anchoring the device to the bone. Thismethod presents the same disadvantage with respect to the amount ofsurface area in contact with the bone as described in connection withthe Harwin, et. al. patent, supra.

[0015] The Hayhurst patent further describes an approach to anchoring asuture to bone using an elongated anchor member shaped to normallyassume a straight configuration which is then bent or flexed to allow itto be inserted through a needle or lumen and then expelled such that itreturns to its straight configuration in a position generallyperpendicular to the suture. This approach is designed for applicationsin which the anchor member may be placed between cartilage and bone andis impractical for use where the suture must be anchored directly to thebone—the applications for which the present invention is specificallydesigned.

[0016] Other similar approaches are described in U.S. Pat. No. 5,417,712to Whittaker, et al. This patent describes anchor devices using variousdifferent barbs and wings to secure the anchor members to the bone. Thisapproach, however, suffers the disadvantage of a small surface areadisposed against the bone and a relatively weak construction andresultant anchoring interface.

[0017] Bone anchor designs utilizing a means of disposing an anchoringdevice below the cortical bone in a generally parallel position to thecortical bone and in a perpendicular position to the suture aredescribed in U.S. Pat. No. 5,941,900 to Bonutti and in U.S. Pat. No.6,045,574 to Thal. These designs use a hole in the cortical bone throughwhich an anchor is inserted. The hole is drilled such that the shorteraxis of the anchor will fit through the diameter of the hole, with thelonger axis of the anchor being parallel to the axis of the drilledhole. After deployment in to the cancellous bone, the anchor is rotated90° so that the long axis is aligned perpendicularly to the axis of thehole. The suture is pulled, and the anchor is seated up against theinside surface of the cortical layer of bone. Due to the mismatch in thedimensions of the long axis of the anchor and the hole diameter, theanchor cannot be retracted proximally from the hole, thus providingresistance to pull-out.

[0018] These anchors, however, do not have the ability to be bent orflexed for deployment through a narrow lumen or hypotube, makinginsertion and placement difficult. They also suffer from the samedisadvantage of a small surface area to be disposed against the corticalbone as the other applications described above.

[0019] U.S. Pat. No. 6,146,406 to Shluzas et al. discloses a bone anchorhaving first and second anchoring legs and a bridge joining theanchoring legs between their proximal and distal ends. Portions of theanchoring legs on a proximal side of the bridge are configured toelastically compress together in response to an insertion force appliedto the bone anchor during insertion of the bone anchor into a bone hole,and to plastically splay apart in response to a withdrawal force appliedto the bone anchor, which force is applied by pulling on the sutureextending proximally from the surgical site. This anchor also has arelatively limited surface area contact with the lower surface of thecortical bone and with the surrounding cancellous bone, and can bedifficult and tricky to insert and deploy.

[0020] What is needed, therefore, is a new approach for repairing therotator cuff or fixing other soft tissues to bone, wherein the sutureresides completely below the cortical bone surface, there is norequirement for the surgeon to tie a knot to attach the suture to thebone anchor, and wherein the procedure associated with the new approachis better for the patient, saves time, is uncomplicated to use, andeasily taught to practitioners having skill in the art.

SUMMARY OF THE INVENTION

[0021] The present invention overcomes the disadvantages of prior artdevices and provides further advantages by utilizing the difference indensity in the cortical bone (the tough, dense outer layer of bone) andthe cancellous bone (the less dense, airy and somewhat vascular interiorof the bone). There is a clear demarcation between the cortical bone andcancellous bone, where the cortical bone presents a kind of hard shellover the less dense cancellous bone.

[0022] A major aspect of the present invention is to provide a means toeither attach a suture securing device to the inventive anchoringdevice, or to attach a suture directly to the inventive device outsidethe body, then deploy the entire apparatus into the procedural areathrough a lumen in a tube. Once inserted into the procedural area withinthe bone, the device is expanded to anchor it beneath the cortical layerof bone. When the device is deployed, it extends radially into thecancellous bone just beneath the cortical layer of bone at the point atwhich the cortical and cancellous layers of bone meet. The manner inwhich the present invention is designed prevents it from returning,after it has been deployed, to the folded or bent profile it assumed asit was being deployed. This design, moreover, prevents the inventionfrom moving proximally due to the density of the cortical bone againstwhich it is seated, or from moving either distally or radially due tothe amount of anchor surface area which is extended into the cancellousbone. This approach is practicable for use in an arthroscopic procedureand eliminates the disadvantages associated with the use of screws,tacks, and staples described above. The present invention solves theproblems outlined above by providing innovative bone anchor andconnective techniques which permit a suture attachment which liesbeneath the cortical bone surface, without the necessity of tying knots.

[0023] More particularly, there is provided in a preferred embodiment abone anchor device for attaching connective tissue to bone, whichcomprises disk adapted for insertion into a portion of bone. The disk ismovable between a bent orientation for presenting a smallercross-section and an expanded orientation for presenting a largercross-section, and the disk is substantially planar when in the expandedorientation. The bent orientation is utilized for inserting the diskthrough a small hole into a region of cancellous bone beneath thecortical bone layer, after which the disk is actuated to move into itsexpanded orientation so that it will be permanently anchored in thecancellous bone, as it will be too large to return proximally throughthe hole in the cortical bone layer. The disk is generally ellipticalwhen in the expanded orientation, and presents a generally circularfootprint when in the bent orientation and viewed from a proximalposition.

[0024] In one preferred embodiment, the substantially planar disk isannular, comprising an annular sidewall and a center aperture. Such anembodiment is particularly useful with a separate suture retaininganchor disposed distally of the disk. Two axial suture receiving groovesdisposed on an inner surface of the annular sidewall, spaced from oneanother by approximately 180 degrees, are preferably employed.

[0025] In another embodiment, wherein the disk itself may be utilized asthe suture retaining anchor, the substantially planar disk issubstantially solid, having two small apertures adjacent to one anotherin a center portion thereof for receiving suturing materialtherethrough.

[0026] A slit is preferably disposed in the disk for facilitating themovement of the disk between the bent orientation and the expandedorientation, and, more preferably, two such slits, spaced approximately180 degrees apart, are employed. The disk has a longitudinal axisextending between a proximal end and a distal end thereof, wherein thedisk bends about an axis which lies transversely to the longitudinalaxis. The disk forms a generally “V” shape in the bent orientation. In apreferred embodiment, each slit comprises an axial portion extendingfrom the distal end of the disk, and a circumferential portion extendingabout a portion of an outer sidewall of the disk, wherein thecircumferential portion is in communication with the axial portion sothat the two slit portions together form each generally “T” shaped slit.A thin axial length of the sidewall extends between the proximal end ofthe disk and the circumferential slit portion. The disk bends about thetransverse axis in a region including the thin axial length of each ofthe two slits. In one embodiment, wherein the disk is formed of flatstock resilient material, such as spring steel, tension applied toopposing edges of the disk cause the bending to occur, because thenatural orientation of the disk is its expanded planar configuration. Inanother embodiment, however, wherein the disk is formed from tubularstock, which is a non-resilient material, such as stainless steel, anaxial compressive force applied to the disk causes the bending to occur.In this configuration, the natural orientation of the disk is its bent,reduced configuration, and the axial compressive force is applied toforce the disk to its expanded flat configuration.

[0027] In preferred embodiments, the disk has a thickness ofapproximately 0.031 inches and the thin axial length of the sidewall isapproximately 0.006 inches long. As noted supra, in one embodiment, itcomprises spring stainless steel, and is biased by the spring stainlesssteel to assume the expanded orientation unless otherwise constrained.In a second embodiment it comprises ordinary stainless steel or othersuitable biocompatible material, and must be forced into the expandedorientation.

[0028] In another embodiment, designed to substantially increase thepull-out strength of the anchor, a plurality of the aforementioneddisks, arranged in a stacked array, are employed.

[0029] In another aspect of the invention, there is provided a boneanchor apparatus, which comprises a first tube, a second tube coaxiallyand slidably disposed within the first tube, and a disk which is movablebetween a bent orientation for presenting a smaller cross-section and anexpanded orientation for presenting a larger cross-section. Duringdeployment of the bone anchor, the disk is disposed within the firsttube distally of the second tube, in the aforementioned bentorientation, with a distal end of the second tube engaging the disk. Inthe spring steel embodiment, tension applied to opposing edges of thedisk by an inner wall of the first tube cause the bending to occur. In apreferred embodiment, the first tube comprises a proximal end portionhaving a first diameter and a distal end portion having a seconddiameter which is reduced relative to the first diameter. An axiallength of the distal end portion is approximately equal to a thicknessof cortical bone in a portion of bone into which the disk is to bedisposed to function as a bone anchor, wherein a transition region onthe tube between the proximal and distal end portions is adapted tofunction as a stop when the first tube is inserted into a hole in thebone portion, thereby ensuring that a distal end of the first tube isdisposed in cancellous bone beneath the cortical bone thickness.

[0030] Preferably, there is disposed a slit in an outer wall of thefirst tube, which slit extends proximally from the distal end of thefirst tube proximally of the transition region. Additionally, there is aslit in an outer wall of the second tube, wherein the first and secondtubes are rotationally oriented relative to one another, when the secondtube is disposed within the first tube, so that the slits in each of thefirst and second tubes are substantially coincident with one another.

[0031] In still another aspect of the invention, there is provided abone anchor apparatus which comprises an anchor body having a firstdisplaceable portion and a second displaceable portion, together with aconnecting portion which joins the first and second displaceableportions. Advantageously, the first and second displaceable portions areeach moveable from a first orientation wherein portions of each of thefirst and second displaceable portions are disposed proximally of theconnecting portion, and a second orientation wherein the first andsecond displaceable portions and the connecting portion all lie insubstantially the same plane. Preferably, the first and seconddisplaceable portions in combination with the connecting portioncomprise a disk, and a suture receiving groove is disposed in each ofthe first and second displaceable portions. In a presently preferredembodiment, the anchor body is initially disposed in the firstorientation.

[0032] In yet another aspect of the invention, there is disclosed amethod for securing connective tissue to bone. The inventive methodcomprises steps of securing a first end of a length of suture to aportion of soft tissue to be attached to a portion of bone, andthreading a second end of the length of suture through an aperture in abody of a bone anchor disk. The bone anchor disk is disposed within alumen of a tube, with the disk being disposed in a bent orientationhaving a reduced cross-section. A distal end of the tube is insertedinto a hole within the portion of bone. The disk is then deployed fromthe distal end of the tube. Once deployed, the disk moves to an expandedorientation, so that the disk becomes anchored within the portion ofbone.

[0033] In still another aspect of the invention, there is disclosed amethod of fabricating a bone anchor device. The inventive methodcomprises steps of providing a tube of biocompatible material, forming abone anchor device by making a series of cuts on a first end of thetube, and separating the bone anchor device from a remaining portion ofthe tube by making a further cut through the tube.

[0034] The invention, together with additional features and advantagesthereof, may best be understood by reference to the followingdescription taken in conjunction with the accompanying illustrativedrawing.

BRIEF DESCRIPTION OF THE DRAWINGS

[0035]FIG. 1 is a perspective view of a presently preferred embodimentof the inventive bone anchor device, shown in a fully expandedconfiguration;

[0036]FIG. 2 is a perspective view similar to that of FIG. 1,illustrating the inventive bone anchor device in a folded configuration;

[0037]FIG. 3 is a proximal plan view of the inventive bone anchor devicewherein tension has been applied to each end of the device so that it isheld in a circular profile;

[0038]FIG. 4 is a proximal plan view of the inventive bone anchordevice, similar to that of FIG. 3, wherein tension is no longer appliedto each end of the device, so that it re-assumes an elliptical shape;

[0039]FIG. 5 is a perspective view illustrating a preferred apparatusand method for inserting the inventive bone anchor device;

[0040]FIG. 6 is a schematic view, in cross-section, illustrating apreferred method for deploying the inventive bone anchor device;

[0041]FIG. 6A is a cross-sectional view of the area identified by thecircle labeled 6A in FIG. 6, showing insertion of the inventive boneanchor device into a suitable bone site;

[0042]FIG. 6B is a cross-sectional view similar to FIG. 6A showing thebone anchor device after deployment;

[0043]FIG. 7 is a perspective view of an alternative embodiment of theinventive anchor device, which may be utilized without an associatedsuture securing device;

[0044]FIG. 8a is a plan view, in cross-section, of an alternativeembodiment of the inventive anchor device, wherein a plurality ofstacked elliptical disks are utilized rather than a single ellipticaldisk, as in the embodiments of FIGS. 1-7;

[0045]FIG. 8b is a top (proximal) view of the embodiment of FIG. 8a;

[0046]FIG. 9a is plan view, similar to FIG. 8a, of yet anotheralternative embodiment of the inventive anchor device;

[0047]FIG. 9b is a top (proximal) view of the embodiment of FIG. 9a;

[0048]FIG. 10 is a perspective view of a tube of suitable material forfabricating an embodiment of the inventive anchor device using analternative fabrication method;

[0049]FIG. 11 is a perspective view similar to FIG. 10, illustrating thetube after a first fabrication step has been performed;

[0050]FIG. 12 is a perspective view similar to FIGS. 10 and 11illustrating the tube after a second fabrication step has beenperformed;

[0051]FIG. 13 is a perspective view similar to FIGS. 10-12 illustratingthe tube after a third fabrication step has been performed;

[0052]FIG. 14 is a perspective view from one end of the inventive anchordevice fabricated from the tube shown in FIG. 10; and

[0053]FIG. 15 is a perspective view from the side of the inventiveanchor device of FIG. 14.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0054] Referring now more particularly to the drawings, there is shownin FIG. 1 a bone anchor 10 constructed in accordance with an embodimentof the present invention, comprised of an elliptical disk 12 with agenerally circular aperture 14 in its center. In this first embodiment,the disk 12 is fabricated of flat stock, preferably 301 stainless springsteel, or other biocompatible equivalent material, and has a thicknessof approximately 0.031 inches. First and second slits 16 a and 16 b,respectively, formed in a generally “T” shape when viewed from the side,are cut into each side of the annular disk from its distal end, usingelectro-discharge machining (EDM) techniques, or the like, and arespaced approximately 180 degrees from each other about the periphery ofthe disk. The “T” shaped slits 16 a, b are cut entirely through theannular sidewall 17 of the disk 12, and function to allow the disk to bebent in an upward or proximal direction for deployment into a portion ofbone, as shall be more particularly described in connection with FIG. 2,below, and also to prevent “bend-back” when the disk returns to its flator unfolded configuration (meaning that the slits will assist inpreventing the disk from over-bending into a downward or distaldirection as it returns to its unfolded configuration). The circularaperture 14 has first and second axially oriented grooves or channels 18a and 18 b, respectively, in its inside surface 19, which are preferablyspaced approximately 180 degrees apart and are offset about 90 degreesfrom each slit 16 a, b. The aperture 14 permits the deployment of asuture securing apparatus into the desired bone structure distallythrough the inventive device, and also receives and permits passage ofsuture material therethrough.

[0055] In FIG. 2 the elliptical disk 12 has been bent upward orproximally into what might be described as a generally “V” shape byexerting tension on each end of the disk at locations about 90 degreesdisplaced from each of the “T” shaped slits 16 a, b. Such appliedtension, the application of which in the illustrated embodiment will bediscussed in greater detail hereinbelow, causes the thinner area 20 a,20 b of the proximal end of the disk formed as a result of the presenceof the T shaped slits 16 a, 16 b, which is preferably fabricated to havea thickness of approximately 0.006 inches from the proximal end of the Tshaped slit to the proximal end of the disk 12, to bend about an axis X(FIG. 3), which axis lies generally transversely to a longitudinal axisY (FIG. 5) for as long as such tension is continually exerted. When thetension is released, the spring-like action of the thinner profileformed at the proximal ends of such “T” shaped slits 16 a, b acts tocause the disk to return to its original flat profile.

[0056]FIG. 3 is a proximal view of the inventive device as it appearswith tension being applied to each end of the elliptical disk asdescribed in connection with FIG. 2, above. It can be seen from FIG. 3that applying such tension to the disk 12 causes it to be held in acircular profile. This circular profile allows the device to be insertedinto a length of hypotubing for deployment arthroscopically into thedesired surgical area by means of a trocar. The device is insertedthrough a length of hypotubing such that it is deployed at the juncturebetween the cancellous and cortical bone structures as shall be morefully illustrated hereinbelow.

[0057]FIG. 4 is a proximal view of the inventive device as it appearsonce the referenced tension is no longer applied to each end of theelliptical disk 12. It can be seen from FIG. 4 that once the tension isreleased, the disk 12 springs back to its original elliptical shape asviewed from a proximal direction as well as to its original flat profileas viewed from the side. As the disk 12 returns to its original profile,the two ends of the elliptical disk are pushed into the cancellous bonestructure just below the point where the cancellous bone meets thecortical bone. When the disk 12 is returned to its original flatprofile, its profile as viewed from a proximal direction returns from around to an elliptical profile. Accordingly, with such a profile, thedisk 12 is larger in cross-section than is the cross-sectional width ofthe hole in the bone structure into which it is inserted, such that thedevice 10 is anchored against the cortical bone in much the same waythat a “moly” bolt becomes anchored within a wall or ceiling when it isradially expanded after insertion into the wall or ceiling through adrilled hole. The method by which the device is anchored to the bonestructure shall be more fully described and illustrated in conjunctionwith FIGS. 5 & 6 below.

[0058] Referring now to FIG. 5, a presently preferred apparatus by whichthe bone anchor 10 is deployed into desired bone structure ( in thepreferred case, a humeral head) to secure soft tissue to bone will bedescribed. Initially, a suture 24, is stitched in a suitable manner tothe soft tissue to be repaired (preferably, a rotator cuff tendon, whichis not shown in this figure). The stitching process may be accomplishedby any known means, and any known suture stitch may be employed, theobjective being to employ a secure stitch so that the suture is notinadvertently separated from the tendon after completion of the repairprocedure, necessitating re-entry to the surgical site. In preferredapproaches, the suture is attached to the soft tissue using a “mattressstitch”, which is well known in the art as being a particularly securestitch which is unlikely to fail postoperatively.

[0059] Of course, as discussed supra, the preferred repair procedurediscussed herein is an arthroscopic procedure, wherein an initial accessincision is made to the repair site, and a trocar 25 is inserted intothe access incision to provide access to the repair site for surgicalinstruments as well as optical instruments. Preferably, a suturinginstrument is inserted into the trocar to perform the aforementionedsuturing step. Of course, the inventive device may also be utilized inan open surgical procedure, if desired, wherein the sutures are manuallyplaced.

[0060] Once the suturing process is completed, the free ends 26 of thesuture 24 are removed proximally through the trocar 25 from thepatient's body, together with the suturing instrument. The free ends 26of the suture 24 may then be attached to a suture anchoring device inthe patient's body, which device may be integral with the bone anchor 10or separate therefrom. The specifics of such suture anchoring systemsare beyond the scope of the present invention, so, for the purposes ofthis description, a simple cylindrical suture anchoring device 28through which the free ends 26 of the suture 24 have been threaded isshown.

[0061] Once the free ends 26 of the suture 24 are threaded through thesuture securing device 28, they are threaded proximally through theaperture 14 in the bone anchor 10. The grooves 18 a, 18 b are useful forreceiving the suture which passes through the aperture 14. The suturesecuring device 28 and bone anchor 10 are then inserted distally into alength of hypotubing 30 which includes a reduction in diameter at itsdistal end 31 so that its distal end is narrower than its proximal end32. The narrower distal end 31 of the hypo tube 30 is adapted to fitinto a hole which has been drilled into the bone structure (not shown inFIG. 5) such that the distal end of the hypotube will be disposed at adepth approximately equal to the depth of the cortical bone andcancellous bone interface. In other words, the length of the narrowerdistal end 31 of the hypo tube 30 is predetermined to coincide with theapproximate thickness of the outer cortical layer of bone, so that theportion of tubing which is stepped outwardly from the smaller diameterof the distal end of the tube to the larger diameter of the proximal endof the tube acts as a stop, thereby ensuring that the anchor 10 will bedisposed at the approximate junction of cortical and cancellous bone. Aslit 33 is disposed in the distal end of the hypotube 30 to allow thehypotube 30 to be inserted into the hole disposed in the bone withoutinterfering with the bound end of the suture 24 which has been stitchedthrough the rotator cuff.

[0062] In one method of the present invention, a mandrel 34, made from anarrower length of hypotubing than the notched hypotube 30, is inserteddistally into the hypotube 30 proximally from the bone anchor 10. Themandrel 34 has a rounded distal end that fits into and engages theproximal end of the disk 12 when the disk 12 is held into theaforementioned generally “V” shape as a result of the tension applied toits ends by the inside wall of the hypotube 30. A slit 35 is disposed inthe distal end of the mandrel 34, in alignment with the correspondingslit 33 in the hypotube 30 when the mandrel 34 is inserted coaxiallyinto the hypotube 30. Again, the slits 35 and 33 function to prevent theapparatus from interfering with the bound ends of the suture 24 as theapparatus is inserted into the hole in the bone structure. It is notedthat the free ends 26 of the suture 24 pass proximally from the suturesecuring device 28, through the bone anchor 10 and mandrel 34 and out ofthe body, so that they may be manipulated by the practitioner performingthe procedure.

[0063] The entire apparatus, consisting of the hypotube 30 with thesuture securing device 28, the bone anchor device 10, and the mandreldevice 34, all disposed coaxially within the hypotube 30, can now beinserted distally through the trocar 36 into the desired surgical site,such as, preferably, the shoulder of a patient.

[0064] To deploy the bone anchor 10 through the hypotube 30, the mandrel34 is pushed in a distal direction against the bone anchor 10, pushingthe bone anchor 10 out of the hypotube 30 and into the bone structure.When the bone anchor 10 is pushed completely out of the hypotube 30, sothat tension is no longer applied to the ends of the elliptical disk 12by the internal surface of the hypotube 30, the disk 12 returns from thegenerally “V” shaped profile exhibited while inside the hypotube 30(FIGS. 2 and 3) to its original flat profile (FIGS. 1 and 4). Thiscauses the ends of the elliptical disk 12 to push or dig into the softcancellous bone just below the surface of the cortical bone layer.

[0065] Once the disk 12 along with the suture securing device 28 havebeen inserted into the bone structure, the hypotube 30 and mandrel 34are removed through the trocar 25 out of the body. The free ends 26 ofthe suture 24 are then pulled in a proximal direction by the surgeon, inorder to permit the soft tissue which is being reattached to adjacentbone structure to be adjusted positionally as necessary. This will alsoexert a distal force on the disk 12, which force acts to secure the diskin position against the cortical bone and to further secure the disk inits flat profile. As described in connection with FIG. 3, above, theflat profile of the disk 12 is larger than the diameter of the hole 42,making it very difficult or impossible to pull the disk proximally outof the bone structure.

[0066] In FIGS. 6, 6A, and 6B, there is shown a cross-sectional view ofa human shoulder 40 on the left side of the body as seen from the frontof the body and which illustrates a rotator cuff tendon 44 which isdisposed across a humeral head 46. It is to be understood that, in thisillustration, the rotator cuff tendon 44 is not attached to the humeralhead 46 at the interface 48 between the two. The humeral head 46 iscomprised of an outer surface of cortical bone 49 and inner cancellousbone 50. In one method of use of the above described inventive anchor 10and associated apparatus, the anchor 10 is utilized to assist in therepair of the shoulder 40 by reattachment of the rotator cuff tendon 44to the humeral head 46.

[0067] To that end, as described supra, a trocar 25 is first insertedinto the shoulder in proximity to the area where the rotator cuff tendon44 is to be reattached to the humeral head 46, to allow for arthroscopicaccess. A hole 51 has been made, preferably by drilling or punching, inthe desired location through the cortical bone 49 and into thecancellous bone 50. This illustration is intended only to provide asimple structural overview of the physiological elements involved in atypical situation where it is to be desired that soft tissue such as therotator cuff tendon 44 be reattached to a humeral head 46.

[0068] Referring in particular to FIG. 6B, the bone anchor 10 is shownin its fully deployed state. The disk 12 is in its original flat profilejust below the cortical bone 49 and inserted into the cancellous bone50. The suture 24 is stitched through the rotator cuff tendon 44,threaded through the suture securing device 28, and the bone anchor 10,and then the loose ends 26 of the suture 24 pass through the trocar 25and out of the patient's body. Proximal tension may be applied by thepractitioner to the free ends 26 of the suture 24, to thereby secure thebone anchor device 10 against the cortical bone 49 and prevent the boneanchor device 10 from being removed from the bone structure.

[0069]FIG. 7 illustrates an alternative embodiment of the presentinvention wherein the anchor device 10 may be utilized without anyindependent suture securing device, such as suture anchoring device 28shown in FIGS. 5 and 6. In this embodiment, rather than employing asingle central aperture 14, two smaller apertures 14 a, 14 b areemployed. A length of suture 24 may be threaded through the apertures 14a, 14 b such that a portion 24 a of the suture 24 may be pulled snuglyagainst a distal surface 52 of the disk 12, thereby securing the sutureto the disk 12. The two free ends 26 of the suture 24 may be knotted orotherwise secured together proximally of the anchor device 1 and theexcess suture may then be cut and removed.

[0070] Referring now to FIGS. 8a and 8 b, wherein like elements aredesignated by like reference numerals, preceded by the numeral “1”, afurther alternative embodiment of the present invention is illustrated.In these figures it can be seen that a stack of elliptical springs ordisks 112 are utilized in place of the single elliptical disk employedin the previous embodiments, to together form the bone anchor device110. It should be noted that the thickness of a single disk 112,approximately 0.031 inches in the preferred embodiments, is adequate toresist sufficient “pull-out” forces to be a useful anchor when usedalone, but in certain applications it may be desirable to employ a stackof disks 112 in order to attain substantially greater resistance topull-out forces. The elliptical springs 112 are held in a circularprofile, like the single disk 12 in FIG. 2, by being inserted into alumen 130 of a tube 132, so that the tube forces the disks into thecircular profile. The stack of disks 112 is pushed distally through thelumen 130 by a mandrel 134 and is thereby deployed at the distal edge ofthe cortical bone in the same manner as described in connection with theembodiment of FIGS. 5 and 6 above. This embodiment is intended to bedeployed using a suture anchoring device 128, as in FIG. 5, supra,though any type of suture attachment system could be employed ifdesired. FIG. 8b shows a top view of the embodiment, illustrating theround profile of the elliptical springs in their undeployed state, whilestill within the lumen 130.

[0071] In FIGS. 9a and 9 b, yet a third alternative embodiment is shownwhich is virtual identical to that shown in FIGS. 8a and 8 b except thatthe device herein shown may be utilized without an independent suturesecuring device 128 as is the case with respect to the alternativeembodiment shown in FIGS. 8a and 8 b. In this embodiment, asillustrated, like elements to those of FIGS. 1-8 b are designated bylike reference numerals, preceded by the numeral “2”. The suture 224 issecured directly by the bone anchoring device 210, by looping the suturethrough the suture holes 214 a and 214 b, as illustrated.

[0072] FIGS. 10-15 illustrate an alternative and more cost effectivemethod for fabricating a bone anchoring device of the type disclosed inthis patent application. In general, the bone anchor 310 as fabricatedusing the method of manufacturing to be described is similar in allrespects to the bone anchor 10 as shown in FIGS. 1-7, except that, sinceit is fabricated from tubing, rather than from flat stock, its naturalorientation is the bent orientation similar to that shown in FIG. 2.Once it has been inserted into suitable bone, an actuation device or thesuture itself may be utilized to actuate the anchor 310 to its flat orunfolded deployed orientation.

[0073] More particularly, to fabricate the anchor 310 in accordance withthe inventive method, a tube 360 of suitable biocompatible material,such as 300 series stainless steel, titanium, or carbon steel, andhaving a longitudinal axis 361, is provided (FIG. 10). As shown in FIG.11, using EDM or other suitable cutting techniques, known to thoseskilled in the art, opposing axial channels 362 a, 362 b, extending froma first end 363 of the tube 360, are formed. Following this, additionalcuts 365 a-365 d are made to remove material from the first end 363 ofthe tube 360, as shown in FIG. 12. The final fabrication of the anchor310 configuration is illustrated in FIG. 13, wherein additional cutshave been made as shown, and in FIG. 14, which illustrates the anchor310 after it has been separated from the remainder of the tube 310 bythe completion of cut 367.

[0074] As is apparent from a comparison of FIGS. 2 and 15, the finishedanchor 310 is substantially identical to the anchor 10, although anentirely different fabrication technique has been utilized. Theadvantage of the methods described in connection with FIGS. 10-15 is adramatically lower cost of production and a substantially increased rateof production. The reason for the reduced cost of production, otherthan, of course, the increased rate of production, which naturallyreduces costs proportionately, is the ability to use cheaper materials,and to minimize material waste. The tube 360 may be utilized tofabricate a number of anchors 310, and there is no need to userelatively expensive spring steel, because the natural orientation ofthe anchor 310, because it is fabricated from tubing 360, is the foldedconfiguration shown in FIGS. 14 and 15. Thus, there is no need to bendthe anchor 310 in order to insert it into the procedural site using theinsertion tube 30. Accordingly, there is no need to utilize a materialwhich is capable of expanding back into its natural state once it hasbeen bent. In contrast, once the anchor 310 is properly positionedwithin the desired bone site, below the cortical bone layer, adeployment instrument or other suitable means may be used to move theanchor 310 proximally against the lower surface of the cortical bone.The force applied against the anchor 310 by the cortical bone as theanchor is moved proximally against it forces the anchor to bend into asubstantially flat configuration, similar to that of FIG. 1, so that theanchor is permanently disposed within the bone to anchor the suturetherein.

[0075] One approach is to deploy the anchor to its extended or flatconfiguration using the suture itself, rather than a separate deploymentinstrument. Thus, as discussed supra in conjunction with the FIG. 1embodiment, once the anchor 310 is in place just beneath the corticalbone, the practitioner performing the procedure will pull the sutureproximally, to approximate the soft tissue to the bone, as desired. Asthe suture is pulled proximally, it will exert a proximal force on theanchor 310, thereby pushing it against the cortical bone and forcing itsdeployment to the deployed, substantially flat orientation.

[0076] It is to be understood that the figures of the bone and anchorsseen above are purely illustrative in nature, and are not intended toperfectly reproduce the physiologic and anatomic nature of the humeralhead as expected to be seen in the human species, nor to limit theapplication of the inventive embodiments to repair of the rotator cuff.The invention is applicable to many different types of proceduresinvolving, in particular, the attachment of connective or soft tissue tobone. Accordingly, although an exemplary embodiment of the invention hasbeen shown and described, it is to be understood that all the terms usedherein are descriptive rather than limiting, and that many changes,modifications, and substitutions may be made by one having ordinaryskill in the art without departing from the spirit and scope of theinvention.

What is claimed is:
 1. A bone anchor device for attaching connectivetissue to bone, comprising a disk which is adapted for insertion into aportion of bone, said disk being movable between a bent orientation forpresenting a smaller cross-section and an expanded orientation forpresenting a larger cross-section, said disk being substantially planarin said expanded orientation.
 2. The bone anchor device as recited inclaim 1, wherein said disk is annular, comprising an annular sidewalland a center aperture.
 3. The bone anchor device as recited in claim 2,and further comprising two axial suture receiving grooves disposed on aninner surface of said annular sidewall, said grooves being spaced fromone another approximately 180 degrees.
 4. The bone anchor device asrecited in claim 1, wherein said disk is substantially solid, having twosmall apertures adjacent to one another in a center portion thereof forreceiving suturing material therethrough.
 5. The bone anchor device asrecited in claim 1, and further comprising a slit disposed in the diskfor facilitating the movement of said disk between the bent orientationand the expanded orientation.
 6. The bone anchor device as recited inclaim 5, wherein said disk has a longitudinal axis extending between afirst end and a second end thereof, said disk bending about an axiswhich lies transversely to said longitudinal axis, and forming agenerally “V” shape in said bent orientation.
 7. The bone anchor deviceas recited in claim 6, wherein said slit comprises an axial portionextending from the first end of the disk, and a circumferential portionextending about a portion of an outer sidewall of said disk, saidcircumferential portion being in communication with said axial portionso that the two slit portions together form a generally “T” shaped slit.8. The bone anchor device as recited in claim 7, and further comprisinga thin axial length of said sidewall extending between the second end ofthe disk and said circumferential slit portion.
 9. The bone anchordevice as recited in claim 8, wherein said disk has a thickness ofapproximately 0.031 inches and said thin axial length of said sidewallis approximately 0.006 inches long.
 10. The bone anchor device asrecited in claim 8, wherein said disk bends about said transverse axisin a region including said thin axial length.
 11. The bone anchor deviceas recited in claim 6, wherein tension applied to opposing edges of saiddisk causes said bending to occur.
 12. The bone anchor device as recitedin claim 6, wherein an axial compressive force applied to said diskcauses said bending to occur.
 13. The bone anchor device as recited inclaim 5, and further comprising a second slit disposed approximately 180degrees from the first slit.
 14. The bone anchor device as recited inclaim 1, wherein said disk comprises spring stainless steel, and isbiased by said spring stainless steel to assume said expandedorientation unless otherwise constrained.
 15. The bone anchor device asrecited in claim 1, wherein said disk is initially formed in said bentorientation.
 16. The bone anchor device as recited in claim 1, andfurther comprising a plurality of said disks, arranged in a stackedarray, for providing a higher pull-out force resistance than is possibleusing a single disk.
 17. The bone anchor device as recited in claim 1,wherein said disk is generally elliptical when in said expandedorientation, and presents a generally circular footprint when in saidbent orientation and viewed from a proximal position.
 18. A bone anchorapparatus, comprising: a first tube; a second tube coaxially andslidably disposed within said first tube; and a disk which is movablebetween a bent orientation for presenting a smaller cross-section and anexpanded orientation for presenting a larger cross-section; wherein saiddisk is disposed within said first tube distally of said second tube, insaid bent orientation, a distal end of the second tube engaging saiddisk.
 19. The bone anchor apparatus as recited in claim 18, wherein saidfirst tube comprises a proximal end portion having a first diameter anda distal end portion having a second diameter which is reduced relativeto said first diameter, an axial length of said distal end portion beingapproximately equal to a thickness of cortical bone in a portion of boneinto which said disk is to be disposed to function as a bone anchor,wherein a transition region on said tube between said proximal anddistal end portions is adapted to function as a stop when said firsttube is inserted into a hole in said bone portion, thereby ensuring thata distal end of the first tube is disposed in cancellous bone beneathsaid cortical bone thickness.
 20. The bone anchor apparatus as recitedin claim 19, and further comprising a slit in an outer wall of saidfirst tube, said slit extending proximally from the distal end of saidfirst tube proximally of said transition region.
 21. The bone anchorapparatus as recited in claim 18, and further comprising a slit in anouter wall of said first tube, extending proximally from a distal end ofthe first tube.
 22. The bone anchor apparatus as recited in claim 21,and further comprising a slit in an outer wall of said second tube, thefirst and second tubes being rotationally oriented relative to oneanother, when the second tube is disposed within the first tube, so thatthe slits in each of said first and second tubes are substantiallycoincident with one another.
 23. The bone anchor apparatus as recited inclaim 18, and further comprising a suture retaining device disposeddistally of said disk.
 24. The bone anchor apparatus as recited in claim18, and further comprising a center aperture in said disk for receivingsuture material therethrough.
 25. The bone anchor apparatus as recitedin claim 18, and further comprising a slit disposed in the disk forfacilitating the movement of said disk between the bent orientation andthe expanded orientation.
 26. The bone anchor apparatus as recited inclaim 25, wherein said apparatus has a longitudinal axis which extendsbetween a proximal end and a distal end of said disk, said disk bendingabout an axis which lies transversely to said longitudinal axis, andforming a generally “V” shape in said bent orientation.
 27. The boneanchor device as recited in claim 26, wherein said slit comprises anaxial portion extending from said distal end of the disk, and acircumferential portion extending about a portion of an outer sidewallof said disk, said circumferential portion being in communication withsaid axial portion so that the two slit portions together form agenerally “T” shaped slit.
 28. The bone anchor device as recited inclaim 27, and further comprising a thin axial length of said sidewallextending between the proximal end of the disk and said circumferentialslit portion.
 29. The bone anchor device as recited in claim 28, whereinsaid disk bends about said transverse axis in a region including saidthin axial length.
 30. The bone anchor device as recited in claim 26,wherein tension applied to opposing edges of said disk by an inner wallof said first tube cause said bending to occur.
 31. The bone anchordevice as recited in claim 25, and further comprising a second slitdisposed approximately 180 degrees from the first slit.
 32. The boneanchor device as recited in claim 18, and further comprising a pluralityof said disks, arranged in a stacked array within said first tube. 33.The bone anchor device as recited in claim 18, wherein said disk isgenerally elliptical when in said expanded orientation, and presents agenerally circular footprint when in said bent orientation and viewedfrom a proximal position.
 34. A bone anchor apparatus, comprising: ananchor body having a first displaceable portion and a seconddisplaceable portion; and a connecting portion which joins said firstand second displaceable portions; wherein said first and seconddisplaceable portions are each moveable from a first orientation whereinportions of each of the first and second displaceable portions aredisposed proximally of the connecting portion, and a second orientationwherein the first and second displaceable portions and the connectingportion all lie in substantially the same plane.
 35. The bone anchorapparatus as recited in claim 34, and further comprising a suturereceiving groove in each of the first and second displaceable portions.36. The bone anchor apparatus as recited in claim 34, wherein the firstand second displaceable portions in combination with the connectingportion comprise a disk.
 37. The bone anchor apparatus as recited inclaim 34 wherein the anchor body is initially disposed in said firstorientation.
 38. A method for securing connective tissue to bone,comprising: securing a first end of a length of suture to a portion ofsoft tissue to be attached to a portion of bone; threading a second endof the length of suture through an aperture in a body of a bone anchordisk; disposing said bone anchor disk within a lumen of a tube, the diskbeing disposed in a bent orientation having a reduced cross-section;inserting a distal end of said tube into a hole within said portion ofbone; and deploying said disk from the distal end of said tube.
 39. Themethod as recited in claim 38, and further comprising a step of movingsaid disk to an expanded orientation after deployment from said tube, sothat the disk becomes anchored within said portion of bone.
 40. A methodof fabricating a bone anchor device, comprising: providing a tube ofbiocompatible material; forming a bone anchor device by making a seriesof cuts on a first end of the tube; and separating the bone anchordevice from a remaining portion of the tube by making a further cutthrough said tube.